List of variants in gene TRAPPC9 reported as likely benign for autosomal recessive non-syndromic intellectual disability

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001160372.4(TRAPPC9):c.3279+4C>T	rs79877357	0.02434
NM_031466.8(TRAPPC9):c.-73G>C	rs767996463	0.00005
NM_001160372.4(TRAPPC9):c.2811-4G>A	rs374826041	0.00004
NM_031466.8(TRAPPC9):c.-153G>C	rs773739324	0.00001

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